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巨噬细胞的共感染调节γ干扰素和肿瘤坏死因子诱导的针对细胞内病原体的激活作用。

Co-infection of macrophages modulates interferon gamma and tumor necrosis factor-induced activation against intracellular pathogens.

作者信息

Black C M, Bermudez L E, Young L S, Remington J S

机构信息

Department of Immunology and Infectious Diseases, Palo Alto Medical Foundation, California 94301.

出版信息

J Exp Med. 1990 Sep 1;172(3):977-80. doi: 10.1084/jem.172.3.977.

Abstract

Co-infection of macrophages (M phi) with Toxoplasma gondii and Mycobacterium avium-intracellulare complex (MAC) has been observed in patients with acquired immunodeficiency syndrome (AIDS). In this study we have demonstrated that co-infected murine M phi respond differently to cytokine stimulation than M phi infected with either of the microorganisms alone. Whereas treatment with interferon gamma (IFN-gamma) activated both single and co-infected groups of M phi to kill T. gondii, treatment with TNF did not influence the rate of MAC growth in co-infected M phi, in contrast with the inhibition of growth observed in MAC-infected M phi. These results suggest that in AIDS patients suffering infection with multiple intracellular pathogens, the ability of cytokines to stimulate microbicidal or static activity in mononuclear phagocytes can be impaired by the presence of more than one of the intracellular organisms.

摘要

在获得性免疫缺陷综合征(AIDS)患者中已观察到巨噬细胞(M phi)被刚地弓形虫和鸟分枝杆菌胞内复合体(MAC)共同感染。在本研究中,我们已证明,与单独感染任一微生物的M phi相比,共同感染的鼠巨噬细胞对细胞因子刺激的反应不同。虽然用干扰素γ(IFN-γ)处理可激活单独感染组和共同感染组的M phi以杀死刚地弓形虫,但与在MAC感染的M phi中观察到的生长抑制相反,用TNF处理并不影响共同感染的M phi中MAC的生长速率。这些结果表明,在感染多种细胞内病原体的AIDS患者中,单核吞噬细胞中细胞因子刺激杀菌或抑菌活性的能力可能会因存在不止一种细胞内生物体而受损。

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